This role involves supporting cell therapy manufacturing processes, leading technology transfers, developing automation, ensuring GMP compliance, and collaborating across departments.

The HR Business Partner serves as the on-site HR resource, providing employee support and managing HR processes in a manufacturing environment while partnering with leadership to ensure compliance and improve HR practices.

Lead the design and optimization of SAP solutions for manufacturing in cell therapy. Ensure compliance with GMP and integrate with supply chains.

The GMP Metrology Specialist manages metrology activities for equipment calibration, ensures compliance with GMP standards, and supports cell therapy manufacturing.

The Manufacturing Supervisor oversees cGMP operations and manages the production of cell therapy products, ensuring compliance, team development, and process optimization.

The Senior Director of IDMO Site Quality leads QA/QC operations for cell therapy manufacturing, ensuring compliance with cGMP while fostering collaboration across departments and stakeholders for successful product outcomes.

Cellares seeks a Senior Scientist in Process Development to execute and analyze experiments for cell therapy, interface cross-functionally, and mentor junior staff.

The Automation Engineer will develop and optimize automated QC workflows, troubleshoot systems, and support laboratory operations in a GMP environment.

The Quality Control Analyst will perform analytical testing, including in-process, lot release, and stability testing while ensuring compliance with cGMP guidelines. They will also investigate discrepancies and support equipment validation and documentation for regulatory submissions.

Lead and stabilize GMP-critical enterprise and manufacturing systems (ERP, MES, QMS, PLM, LIMS), ensure data integrity and traceability, drive integrations, governance, and validation, partner with Manufacturing/Quality/Finance, and provide hands-on leadership to make systems audit-ready and scalable for commercial manufacturing.

The Automation Engineer will develop and optimize lab automation systems, validate QC workflows, and ensure functionality of automated systems for cell therapy manufacturing.

The Director, Operations Finance will oversee FP&A for the Operations organization, driving financial insights, cost forecasts, and operational efficiencies across manufacturing sites globally.

The Director, Corporate FP&A leads financial planning processes, collaborates with functional leaders, and provides analysis to drive financial performance in a biotechnology setting.

Design and implement software subsystems at the software-hardware boundary for a cell therapy manufacturing platform. Maintain system architecture and documentation, support subsystem teams, perform root-cause analysis, and lead verification and validation activities as the product scales from R&D to production.

The Director of Enterprise Programs leads client programs in process development, managing teams, overseeing tech transfer, ensuring compliance, and optimizing manufacturing processes for cell therapies.